Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B3/00—Preparation of cellulose esters of organic acids
  • C08B3/06—Cellulose acetate, e.g. mono-acetate, di-acetate or tri-acetate
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
  • C08L1/08—Cellulose derivatives
  • C08L1/10—Esters of organic acids, i.e. acylates
  • C08L1/12—Cellulose acetate
• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
  • A24D3/00—Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
  • A24D3/06—Use of materials for tobacco smoke filters
  • A24D3/067—Use of materials for tobacco smoke filters characterised by functional properties
  • A24D3/068—Biodegradable or disintegrable
• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24D—CIGARS; CIGARETTES; TOBACCO SMOKE FILTERS; MOUTHPIECES FOR CIGARS OR CIGARETTES; MANUFACTURE OF TOBACCO SMOKE FILTERS OR MOUTHPIECES
  • A24D3/00—Tobacco smoke filters, e.g. filter-tips, filtering inserts; Filters specially adapted for simulated smoking devices; Mouthpieces for cigars or cigarettes
  • A24D3/06—Use of materials for tobacco smoke filters
  • A24D3/08—Use of materials for tobacco smoke filters of organic materials as carrier or major constituent
  • A24D3/10—Use of materials for tobacco smoke filters of organic materials as carrier or major constituent of cellulose or cellulose derivatives
• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24F—SMOKERS' REQUISITES; MATCH BOXES; SIMULATED SMOKING DEVICES
  • A24F13/00—Appliances for smoking cigars or cigarettes
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
  • Y10T428/269—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension including synthetic resin or polymer layer or component
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2913—Rod, strand, filament or fiber
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2913—Rod, strand, filament or fiber
  • Y10T428/2933—Coated or with bond, impregnation or core
  • Y10T428/2964—Artificial fiber or filament
  • Y10T428/2965—Cellulosic

Definitions

• the present invention relates to a molded article of biodegradable cellulose acetate and a filter plug for a smoking article.
• Cellulose acetate is widely used as various molded articles, for example, fibers for tobacco filter materials and for woven fabric for clothes, and as films, as well as molded articles prepared by an injection molding, an extrusion molding, etc.
• Cellulose acetate which is prepared by converting cellulose into an acetic acid ester, is essentially a biodegradable substance. However, the biodegradability of cellulose acetate is not necessarily satisfactory in practice.
• a molded article made of cellulose acetate retains its original shape for 1 or 2 years. It takes a very long time for the molded article to be decomposed completely by biodegradation. These molded articles are handled as waste materials in some cases so as to be used for the land reclamation. In other cases, these molded articles are not recovered so as to be left as they are in the natural environment. It follows that it is very important to accelerate the biodegradability of cellulose acetate.
• biodegradability of cellulose acetate is dependent on DS (Degree of Substitution: the number of acetyl groups per anhydroglucose monomer).
• DS Degree of Substitution: the number of acetyl groups per anhydroglucose monomer.
• the mechanism of biodegradation is considered to be as follows.
• the acetyl group of cellulose acetate is broken by an extracellular enzyme released from bacteria, leading to decrease in the DS value of cellulose acetate. Then, the cellulose acetate having its DS value decreased is readily undergone an enzyme decomposition by cellulase, etc. widely distributed in the environment so as to receive finally a biological metabolism and, thus, to be decomposed into carbon dioxide and water.
• the rate-limiting step of the biodegradation rate is considered to be the initial breakage of the acetyl group.
• Japanese Patent Disclosure (Kokai) No. 6-199901 discloses a method of controlling the biodegradability of cellulose acetate by adding an acid compound having an acid dissociation constant larger than that of acetic acid to cellulose acetate.
• the cellulose acetate chemically brings about a hydrolysis under the influence of the acid compound immediately after the time when the acid compound is added to the cellulose acetate, and the DS value of the cellulose acetate begins to be decreased. Since the DS value of the cellulose acetate composition (article) having the acid compound added thereto is thus decreased with time, it is impossible to maintain the DS value of the starting cellulose acetate.
• the DS value of cellulose acetate greatly affects the function of the cellulose acetate article.
• a filter for tobacco When it comes to, for example, a filter for tobacco, the taste of the tobacco is greatly changed by the change in the DS value of cellulose acetate.
• the DS value of cellulose acetate used as a filter for tobacco it is quite undesirable for the DS value of cellulose acetate used as a filter for tobacco to be changed with time from the design value under the ordinary environment, up to the time when the tobacco is smoked.
• the chemical hydrolysis of the acetyl group of cellulose acetate occurring in the presence of the acid compound produces acetic acid with progress of the chemical hydrolysis, i.e., with decrease in the DS value of cellulose acetate.
• the acetyl group eliminated from cellulose acetate is liberated as acetic acid.
• the liberated acetic acid imparts a strong acetic acid odor to the cellulose acetate article.
• the acetic acid odor is not a desirable factor in various articles. In the case of, for example, a filter for tobacco, the acetic acid odor markedly deteriorates the taste of tobacco.
• an object of the present invention is to provide a means for accelerating the biodegradability of cellulose acetate, which permits suppressing the change with time in the DS value of cellulose acetate and also permits suppressing the generation of the acetic acid odor.
• the present inventors have found that, by complexing a certain decomposition accelerating agent which accelerates the decomposition of cellulose acetate with a certain reaction controlling agent which suppresses the decomposition reaction of cellulose acetate, the decomposition accelerating function of the decomposition accelerating agent can be suppressed under the ordinary use conditions of cellulose acetate, but the composite material dissociates its complexed state only when the cellulose acetate is brought into contact with water, to liberate the reaction controlling agent within the composite material, thereby allowing the decomposition accelerating agent to exhibit its decomposition accelerating function.
• cellulose acetate having contained therein, a composite material of a decomposition accelerating agent consisting of at least one compound selected from the group consisting of oxygen acid of phosphorus, oxygen acid of sulfur, oxygen acid of nitrogen, a partial ester or hydrogen salt of these oxygen acids, carbonic acid and its hydrogen salt, a sulfonic acid, and a carboxylic acid with a reaction controlling agent consisting of at least one compound selected from the group consisting of a nitrogen-containing compound, a hydroxy compound, an oxygen-containing heterocyclic compound, and a sulfur-containing heterocyclic compound.
• a decomposition accelerating agent consisting of at least one compound selected from the group consisting of oxygen acid of phosphorus, oxygen acid of sulfur, oxygen acid of nitrogen, a partial ester or hydrogen salt of these oxygen acids, carbonic acid and its hydrogen salt, a sulfonic acid, and a carboxylic acid
• a reaction controlling agent consisting of at least one compound selected from the group consisting of a nitrogen-containing compound, a hydroxy
• the cellulose acetate composition of the present invention containing cellulose acetate and a composite material, contained in the cellulose acetate, of the decomposition accelerating agent with the reaction controlling agent permits suppressing the change with time in the DS value of the cellulose acetate. Therefore, the composition of the present invention permits maintaining the article performance as designed and also permits suppressing the acetic acid odor.
• the cellulose acetate composition of the present invention provides a molded article that begins to be decomposed only when the article is brought into contact with water.
• the cellulose acetate composition of the present invention is provided as a molded article such as fibers.
• a filter plug for tobacco comprising cellulose acetate fibers, characterized in that each of the cellulose acetate fibers contains, in at least a surface region thereof, a composite material of a decomposition accelerating agent consisting of at least one compound selected from the group consisting of oxygen acid of phosphorus, oxygen acid of sulfur, oxygen acid of nitrogen, a partial ester or hydrogen salt of these oxygen acids, carbonic acid and its hydrogen salt, a sulfonic acid and a carboxylic acid, with a reaction controlling agent consisting of at least one compound selected from the group consisting of a nitrogen-containing compound, a hydroxy compound, an oxygen-containing heterocyclic compound, and a sulfur-containing heterocyclic compound.
• the cellulose acetate it is desirable for the cellulose acetate to have a DS value of 2.0 to 2.6.
• the decomposition accelerating agent preferably consists of at least one compound selected from the group consisting of phosphoric acid, polyphosphoric acid, phytic acid, starch phosphate, cellulose phosphate, calcium hydrogenphosphate, lecithin and phosphoric acid di-2-ethylhexyl ester; and phosphoric ester of 2-hydroxyethyl methacrylate, phosphoric ester of 2-hydroxyethyl phenyl methacrylate, alkyl phosphoric ester of 2-hydroxyethyl methacrylate, and polymers and copolymers thereof.
• the reaction controlling agent preferably consists of at least one compound selected from the group consisting of a compound having a pyrrolidone structure, a compound having an oxazolidone structure, a compound having an imide structure, a compound having a pyridine structure, a compound having an amine oxide structure, a compound having a pyrazine structure, polyvinyl alcohol or a derivative thereof, alkyl cellulose, hydroxyalkyl cellulose, sucrose fatty acid ester, propylene glycol fatty acid ester, sorbitan fatty acid ester, glycerin fatty acid ester, polyoxyethylene glycerin fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene sorbitol fatty acid ester, polyoxyethylene fatty acid amide, and fatty acid alkanol amide.
• the decomposition accelerating agent is contained in an amount of 0.01 to 40% by weight based on the cellulose acetate amount, and/or the reaction controlling agent is contained in an amount of 0.01 to 50% by weight based on the cellulose acetate amount.
• the cellulose acetate used in the present invention may be any cellulose acetate, and its DS value is not particularly limited.
• cellulose diacetate having a DS value of 2.0 to 2.6, or cellulose triacetate having a DS value larger than 2.6 can be used.
• cellulose acetate having a DS value 2.0 or less, which has a high biodegradability may be used.
• the composite material contained in cellulose acetate according to the present invention is the one prepared by complexing a predetermined decomposition accelerating agent with a predetermined reaction controlling agent by a chemical interaction (e.g., hydrogen bond).
• the decomposition accelerating agent serves to accelerate the chemical hydrolysis of cellulose acetate, and is selected according to the present invention from the group consisting of oxygen acid of phosphorus, oxygen acid of sulfur, oxygen acid of nitrogen, a partial ester or hydrogen salt of these oxygen acids, carbonic acid and its hydrogen salt, a sulfonic acid and a carboxylic acid. A mixture of two or more of these compounds can also be used.
• the oxygen acid which is also called an oxoacid or an oxyacid, is an acid in which hydrogen that can be dissociated as a proton is bonded to an oxygen atom, and is preferably represented by a general formula
• E represents phosphorus, sulfur or nitrogen.
• a condensate thereof is included in the oxygen acid.
• the oxygen acid of phosphorus includes phosphoric acid (phosphoric acid used in the present specification represents orthophosphoric acid), pyrophosphoric acid, metaphosphoric acid, polyphosphoric acid and hypophosphorous acid.
• the oxygen acid of sulfur includes sulfuric acid.
• the oxygen acid of nitrogen includes nitric acid and nitrous acid.
• Oxygen acids other than, those mentioned above include, for example, phosphorous acid, hypophosophorous acid and hyponitrous acid.
• a partial ester of the oxygen acid is a compound in which not all of the hydroxyl groups of the oxygen acid are esterified.
• partial esters of the oxygen acid of phosphoric acid include PO(OR)(OH) 2 and PO(OR) 2 (OH).
• the hydrogen salt which is also called acid salt, is a compound containing, at its an electrically positive component of a salt of an oxygen acid, a hydrogen ion capable of replacement by a cation.
• the hydrogen salt includes is salt for a compound in which the salt is in equilibrium with a hydrogen salt in water, as well as complex salts such as phosphate hydroxide.
• the reaction controlling agent forms a composite material together with the decomposition accelerating agent by, for example, a hydrogen bond.
• the agent serves to suppress the decomposing action of the decomposition accelerating agent to decompose cellulose acetate under the ordinary storage conditions, and, when contacted with water, dissociates the complexed state to liberate the decomposition accelerating agent thereby enabling the decomposition accelerating agent to perform its decomposing action.
• the reaction controlling agent used in the present invention is selected from the group consisting of a nitrogen-containing compound, a hydroxy compound, an oxygen-containing heterocyclic compound, and a sulfur-containing heterocyclic compound. A mixture of two or more of these compounds can be used.
• the nitrogen-containing compound is a compound having a nitrogen atom in its structure, and includes, for example, ammonia, amines, amine oxides, amides, urethanes, imides, nitro compounds, nitroso compounds, and nitrogen-containing heterocyclic compounds (compounds containing nitrogen as a member of the heterocyclic ring).
• the hydroxy compound is a compound having a hydroxyl group (—OH), and includes, for example, alcohols (including polyhydric alcohols), polyvinyl alcohols, polyglycerins and sugars.
• the oxygen-containing heterocyclic compound is a compound containing oxygen as a member of the heterocyclic ring
• the sulfur-containing heterocyclic compound is a compound containing sulfur as a member of the heterocyclic ring.
• the decomposition accelerating agent and the reaction controlling agent are contained in the cellulose acetate composition in the form of a complexed state formed by a chemical interaction (e.g., hydrogen bond).
• such a composite material and hence the decomposition accelerating agent and the reaction controlling agent are safe and can be supplied in large amounts at an acceptable price.
• a cellulose acetate solution spun in general from a spinning nozzle by a spinning method.
• the decomposition accelerating agent and the reaction controlling agent used in the present invention it is desirable for the decomposition accelerating agent and the reaction controlling agent used in the present invention to be soluble in a solvent used for dissolving cellulose acetate (such as acetone, methylene chloride/methanol mixed solvent, or dimethyl sulfoxide).
• these decomposition accelerating agent and the reaction controlling agent should preferably be capable of pulverization to such a degree as not to adversely affect the properties of the fiber in the spinning step.
• the decomposition accelerating agent used in the present invention is phosphoric acid, polyphosphoric acid, or its partial ester or hydrogen salt.
• the partial ester or the hydrogen salt preferably include, for example, phytic acid, starch phosphate, cellulose phosphate, calcium hydrogenphosphate, lecithin, phosphoric acid di-2-ethylhexyl ester, phosphoric ester of HEMA (2-hydroxyethyl methacrylate), phenyl phosphoric ester of HEMA, alkyl phosphoric ester of HEMA, and homopolymers and copolymers of phosphoric ester of HEMA, phenyl phosphoric ester of HEMA and alkyl phosphoric ester of HEMA.
• the reaction controlling agent used in the present invention preferably consists of a compound having a pyrrolidone structure (e.g., 2-pyrrolidone, N-methyl-2-pyrrolidone or polyvinylpyrrolidone), a compound having an oxazolidone structure (e.g., 2-oxazolidone, 3-methyl-2-oxazolidone or polyvinyl oxazolidone), a compound having an imide structure (e.g., phthalimide, succinimide, riboflavin or polyvinyl phthalimide), a compound having a pyridine structure (e.g., pyridine, nicotinic acid, nicotinic acid amide or polyvinyl pyridine), a compound having an amine oxide structure (e.g., N-methylmorpholine N-oxide, N-methyl piperidine N-oxide
• a pyrrolidone structure e.g., 2-pyrrolidone, N-
• the biodegradation rate of cellulose acetate and the level of suppressing the acetic acid odor of the molded article by controlling the addition amounts of the decomposition accelerating agent and the reaction controlling agent.
• the addition amount of the decomposition accelerating agent can be set optionally depending on the desired biodegradation rate. For example, where it is intended to accelerate the biodegradation rate, the decomposition accelerating agent should be added in a larger amount. However, in view of the moldability of the resultant cellulose acetate composition, it is desirable to add the decomposition accelerating agent in an amount of 0.01 to 40% by weight based on the cellulose acetate amount. More preferably, the decomposition accelerating agent should be added in an amount of 0.01 to 15% by weight based on the cellulose acetate amount.
• the addition amount of the reaction controlling agent can be determined on the basis of the desired level of suppressing the acetic acid odor. Where, for example, it is intended to suppress the acetic acid odor of the molded article to a higher extent, a larger amount of the reaction controlling agent should be added. However, if the reaction controlling agent is added in an excessively large amount, the moldability of the cellulose acetate composition is lowered. On the other hand, if the addition amount of the reaction controlling agent is unduly small, it can not be expected to obtain a desired effect of suppressing the acetic acid odor. Under the circumstances, the amount of the reaction controlling agent added is preferably 0.01 to 50% by weight, more preferably 0.01 to 25% by weight, based on the cellulose acetate amount. Also, where it is intended to suppress completely the generation of the acetic acid odor from the cellulose acetate molded article, it is desirable to add the reaction controlling agent in an amount that is chemically equivalent or more to the addition amount of the decomposition accelerating agent.
• the cellulose acetate composition of the present invention can be formed into molded articles of various structure by the ordinary methods, except that the cellulose acetate composition of the present invention contains the particular composite material.
• a reaction controlling agent and a decomposition accelerating agent can be added first to a solution of cellulose acetate in a solvent such as acetone or methylene chloride, followed by molding the resultant composition by the ordinary method.
• a reaction controlling agent and a decomposition accelerating agent can be added by melting and mixing into a thermally moldable cellulose acetate containing a plasticizer or the like, followed by molding the resultant composition by the ordinary method.
• cellulose acetate fiber used for a tobacco filter can be prepared, for example, as follows.
• a solution (spinning solution) containing cellulose acetate and a composite material of the present invention is prepared.
• the solvent a single solvent such as methylene chloride or acetone or a mixed solvent of, for example, methylene chloride and methanol can be used.
• the cellulose acetate concentration is generally 15 to 35% by weight, preferably 18 to 30% by weight.
• the decomposition accelerating agent and the reaction controlling agent are contained in the spinning solution in amounts falling within the ranges described previously.
• the spinning solution can be prepared by mixing a solution prepared by dissolving or dispersing the decomposition accelerating agent and the reaction controlling agent in a solvent for cellulose acetate with a solution prepared by dissolving cellulose acetate in a solvent for the cellulose acetate.
• the spinning solution can be prepared by directly adding the decomposition accelerating agent and the reaction controlling agent to the solution of cellulose acetate.
• the cellulose acetate spinning solution thus prepared which contains the composite material of the present invention, is supplied to a spinning nozzle device and spun by a dry spinning method, in which the spinning solution is discharged into an atmosphere of high temperatures, so as to obtain a cellulose acetate fiber. It is possible to employ a wet spinning method in place of the dry spinning method.
• a composite spinning into, e.g., fiber side-by-side or sheath-core type fibers by using a cellulose acetate spinning solution containing the composite material and a cellulose acetate spinning solution that does not contain the composite material, such that at least the cellulose acetate composition containing the composite material papers the fiber surface. Additional additives can also be used together in preparing the spinning solution as far as the characteristics of the spinning solution are not impaired.
• the spinning solution contains a photo-degradation accelerating agent such as titanium oxide
• the photo-degradation accelerating effect is combined with the biodegradation accelerating effect of the present invention so as to further enhance the decomposition of the cellulose acetate composition.
• a dispersing agent for example, an emulsifying agent, a plasticizer, a viscosity controlling agent, etc.
• the cellulose acetate fibers of the present invention constituting the filter plug for tobacco each contain a composite material of the present invention in at least a surface region thereof.
• the cellulose acetate fibers may be in the form of fibril.
• the cellulose acetate fiber is in the form of fibril, it is desirable to use other materials described below or the cellulose acetate of the present invention in the form of usual fiber, together with the fibril.
• the cellulose acetate fibers thus obtained are manufactured into a tobacco filter by the ordinary method.
• the manufacturing method of the filter and the construction of the filter are not particularly limited.
• the tobacco filter can be manufactured as follows.
• the cellulose acetate fibers are made into a tow and, then, opened on a tobacco filter plug-making machine, followed by addition of a plasticizer (e.g., triacetyl glycerin) and subsequently forming the resultant material into the shape of a fibrous rod. Finally, the fibrous rod is cut into pieces of a desired length so as to obtain filter plugs. Incidentally, the total degree of fineness as the fiber bundle is set appropriately so as to facilitate the manufacture of the filter plug.
• a rod-like material can be formed on an ordinary plug making machine by using an nonwoven fabric prepared from short fibers prepared by cutting the cellulose acetate fibers into small pieces having a length of 1 to 100 mm.
• the cellulose acetate fiber of the present invention can be used singly for manufacturing a filter. It is also possible to use the cellulose acetate fiber of the present invention as one component together with other constituting materials for manufacturing a filter.
• Such other constituting materials include, for example, natural or semi-synthesized materials (e.g., pulp, linters, cotton, hemp, viscose rayon, copper ammonia rayon, lyocel, wool or a biodegradable polymer of a microorganism production type like polyhydroxy alkanoate); ordinary synthetic materials (e.g., polyolefin like polypropylene, polyester like polyethylene terephthalate, and polyamide); biodegradable synthetic materials (e.g., polylactic acid, polycaprolactone, polybutylene succinate and polyvinyl alcohol); and photo-degradable materials.
• natural or semi-synthesized materials e.g., pulp, linters, cotton, hemp, viscose rayon, copper ammonia rayon
• These materials can be used in the form of fibers or nonwoven fabrics. In such a case, it is particularly desirable to use a material excellent in biodegradability. It is also possible to use a starch foam as a material excellent in biodegradability, though the starch foam is not a fiber.
• a water-soluble adhesive can be used in place of the plasticizer.
• the cellulose acetate fibers are strongly bonded to each other by melt adhesion.
• the filter for tobacco discarded in the natural environment stably retains the rod shape over a long period of time.
• the bonded points among the cellulose acetate fibers are easily dissociated by a large amount of water (rain, sea water, river water, lake water, etc.) when the filter for tobacco is discarded in the natural environment. As a result, the rod shape of the filter for tobacco is readily collapsed.
• the cellulose acetate fibers put in the natural environment is extended on, for example, a surface region of the soil, leading to a large contact area between the fiber and the environment of the microorganisms, which influences the biodegradation rate, with the result that the biodegradation of the tobacco filter is further accelerated.
• This further enhances the biodegradability of the tobacco filter, in cooperation with the acceleration of the biodegradability by the cellulose acetate of the present invention.
• the cellulose acetate fiber may be in the shape of either a staple or a filament.
• the total degree of fineness of the tows can be set optionally.
• the cross sectional shape of each fiber which is not particular limited in the present invention, may be circular, rectangular, etc.
• a cellulose acetate composition containing the additive noted above and a filter for tobacco are featured as follows. Specifically, the decomposition accelerating agent is stabilized by the chemical interaction (e.g., hydrogen bond) with the reaction controlling agent in the process of manufacturing a molded article of cellulose acetate composition and in the stage of the molded article. As a result, the decomposition accelerating agent does not cause a chemical hydrolysis of the cellulose acetate to take place. It follows that the molded article exhibits the properties of the molded article of the ordinary cellulose acetate not containing the composite material of the present invention.
• the decomposition accelerating agent is stabilized by the chemical interaction (e.g., hydrogen bond) with the reaction controlling agent in the process of manufacturing a molded article of cellulose acetate composition and in the stage of the molded article.
• the decomposition accelerating agent does not cause a chemical hydrolysis of the cellulose acetate to take place. It follows that the molded article exhibits the properties of the molded article of the ordinary cellulose
• the composite material of the decomposition accelerating agent with the reaction controlling agent which is contained in the molded article, releases its interaction due to a large amount of water (rain, sea water, river water, lake water, etc.) so as to set free the decomposition accelerating agent.
• the free decomposition accelerating agent exhibits its function (decomposition accelerating function) for the first time.
• the combined use of the decomposition accelerating agent together with the reaction controlling agent can control the reactivity of the decomposition accelerating agent, which accelerates the biodegradability of cellulose acetate, both within the molded article and in the natural environment.
• the molded article of the present invention does not undergo the chemical hydrolysis of cellulose acetate in the stage wherein it is generally used as a molded article.
• the molded article of the present invention retains the properties (DS) of the starting material of cellulose acetate, and the odor of acetic acid is not generated.
• the molded article of cellulose acetate is biodegradably decomposed prominently in the natural environment by the function of the decomposition accelerating agent dissociated from the reaction controlling agent by contact with water.
• Polyvinylpyrrolidone an average molecular weight (weight average molecular weight; the same apples in the following) of 25,000 was added in an amount of 25% by weight of the cellulose acetate to the solution, which was made uniform by stirring.
• phosphoric acid was added in an amount of 5% by weight of the cellulose acetate, and again stirred to uniformity.
• the resultant cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m. It was confirmed from the film thus obtained that the decomposition accelerating agent and the reaction controlling agent constituting the composite material were uniformly dissolved and dispersed in the film so as not to affect the moldability of the cellulose acetate film.
• 2-pyrrolidone was added in an amount of 25% by weight of the cellulose acetate to the solution, which was made uniform by stirring.
• phosphoric acid was added in an amount of 5% by weight of the cellulose acetate and again stirred to uniformity.
• the resultant cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m. It was confirmed from the film thus obtained that the decomposition accelerating agent and the reaction controlling agent constituting the composite material were uniformly dissolved and dispersed in the film so as not to affect the moldability of the cellulose acetate film.
• N-methylmorpholine N-oxide was added in an amount of 25% by weight of the cellulose acetate amount to the solution, which was made uniform by stirring.
• phosphoric acid was added in an amount of 5% by weight of the cellulose acetate, and again stirred to uniformity.
• the resultant cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m. It was confirmed from the film thus obtained that the decomposition accelerating agent and the reaction controlling agent constituting the composite material were uniformly dissolved and dispersed in the film so as not to affect the moldability of the cellulose acetate film.
• Polyvinyl butyral (an average molecular weight of 2,000) was added in an amount of 25% by weight of the cellulose acetate to the solution, which was made uniform by stirring.
• phosphoric acid was added in an amount of 5% by weight of the cellulose acetate and again stirred to uniformity.
• the resultant cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m. It was confirmed from the film thus obtained that the decomposition accelerating agent and the reaction controlling agent constituting the composite material were uniformly dissolved and dispersed in the film so as not to affect the moldability of the cellulose acetate film.
• Polyvinylpyrrolidone (an average molecular weight of 25,000) was added in an amount of 25% by weight of the cellulose acetate amount to the solution, which was made uniform by stirring.
• polyphosphoric acid was added in an amount of 5% by weight of the cellulose acetate and again stirred to uniformity.
• the resultant cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m. It was confirmed from the film thus obtained that the decomposition accelerating agent and the reaction controlling agent constituting the composite material were uniformly dissolved and dispersed in the film so as not to affect the moldability of the cellulose acetate film.
• 2-pyrrolidone was added in an amount of 25% by weight of the cellulose acetate to the solution, which was made uniform by stirring.
• polyphosphoric acid was added in an amount of 5% by weight of the cellulose acetate and again stirred to uniformity.
• the resultant cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m. It was confirmed from the film thus obtained that the decomposition accelerating agent and the reaction controlling agent constituting the composite material were uniformly dissolved and dispersed in the film so as not to affect the moldability of the cellulose acetate film.
• N-methylmorpholine N-oxide was added in an amount of 25% by weight of the cellulose acetate to the solution, which was made uniform by stirring.
• polyphosphoric acid was added to the system in an amount of 5% by weight of the cellulose acetate and stirred to uniformity.
• the resultant cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m. It was confirmed from the film thus obtained that the decomposition accelerating agent and the reaction controlling agent constituting the composite material were uniformly dissolved and dispersed in the film so as not to affect the moldability of the cellulose acetate film.
• Polyvinyl butyral (an average molecular weight of 2,000) was added in an amount of 25% by weight of the cellulose acetate to the solution, which was made uniform by stirring.
• polyphosphoric acid was added in an amount of 5% by weight of the cellulose acetate and stirred to uniformity.
• the resultant cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m. It was confirmed from the film thus obtained that the decomposition accelerating agent and the reaction controlling agent constituting the composite material were uniformly dissolved and dispersed in the film so as not to affect the moldability of the cellulose acetate film.
• Phosphoric acid was added in an amount of 5% by weight of the cellulose acetate to the solution, which was stirred to uniformity.
• the cellulose acetate solution thus obtained was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m.
• Polyphosphoric acid was added in an amount of 5% by weight of the cellulose acetate to the solution, which was stirred to uniformity.
• the cellulose acetate solution thus obtained was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m.
• This cellulose acetate solution was cast on a glass plate and dried to obtain a cellulose acetate film having a thickness of about 100 ⁇ m.
• the acetic acid odor level of each of the cellulose acetate films obtained in Examples 1-8 and Comparative Examples 1-3 was evaluated.
• the acetic acid concentration was measured by punching out a circular piece (a diameter of 5 cm) from each of the films immediately after the manufacture, which was put in an odor bag and left to stand in a constant temperature chamber of 50° C., followed by measuring the acetic acid concentration within the odor bag one week later by a gas detecting tube method.
• the acetic acid odor level of the film was evaluated by an organoleptic examination method. Table 1 shows the results.
• reaction controlling agent suppresses the generation level of the acetic acid odor derived from the addition of a decomposition accelerating agent. More specifically, it is seen that, in the process of manufacturing a molded article (film) of cellulose acetate and in the stage of the molded article, the decomposition accelerating agent is stabilized by the reaction controlling agent so as to suppress the function of the decomposition accelerating agent. Further, it is seen that the degree of suppressing the decomposition can be set as desired by suitably selecting the kind of the reaction controlling agent used.
• cellulose acetate films Five kinds of cellulose acetate films were prepared as in Example 1, except that the amount of polyvinylpyrrolidone (an average molecular weight of 25,000) added was 5% by weight, 10% by weight, 15% by weight, 20% by weight and 30% by weight, respectively, of the cellulose acetate.
• Cellulose acetate films were prepared as in Example 3, except that N-methylmorpholine N-oxide was added in amounts of 1% by weight, 5% by weight, 10% by weight, 15% by weight, 20% by weight and 30% by weight, respectively, of the cellulose acetate.
• a cellulose acetate film was prepared as in Example 1, except that the addition amount of polyvinylpyrrolidone (an average molecular weight of 25,000) was changed to 10% by weight of the cellulose acetate, and that the addition amount of phosphoric acid was changed to 1% by weight of the cellulose acetate.
• a cellulose acetate film was prepared as in Example 3, except that the addition amount of N-methylmorpholine N-oxide was changed to 1% by weight of the cellulose acetate, and that the addition amount of phosphoric acid was changed to 1% by weight of the cellulose acetate.
• the acidity was evaluated in the case where each of the cellulose acetate films prepared in Examples 1, 3, 5 and 7, and Comparative Examples 1-3 was brought into contact with a large amount of water. Specifically, a circular piece (a diameter of 5 cm) was punched out from the film as formed, and was kept dipped in 100 mL of water for one day at room temperature so as to measure the pH value of the dipping water by an ordinary pH meter. Table 6 shows the results.
• the decomposition accelerating agent exhibits its function without being affected by the reaction controlling agent that is used together in any of the Examples, if contacted with a large amount of water.
• the composite material of the decomposition accelerating agent with the reaction controlling agent contained in the cellulose acetate composition of the present invention release its interaction by a large amount of water so as to liberate the decomposition accelerating agent into free state.
• the present invention provides a cellulose acetate molded article which is capable of suppressing the change with time in the DS value of the cellulose acetate and suppressing generation of an acetic acid odor, and which is also excellent in biodegradability.

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